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About This Item
Linear Formula:
C6H5NHCOCH2Cl
CAS Number:
Molecular Weight:
169.61
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
97%
mp
136-139 °C (lit.)
functional group
amide
chloro
SMILES string
ClCC(=O)Nc1ccccc1
InChI
1S/C8H8ClNO/c9-6-8(11)10-7-4-2-1-3-5-7/h1-5H,6H2,(H,10,11)
InChI key
VONWPEXRCLHKRJ-UHFFFAOYSA-N
General description
2-Chloro-N-phenylacetamide, also known as chloroacetanilide, can be prepared by reacting aniline with chloroacetylchloride in glacial acetic acid. The analysis of its crystal structure shows the presence of N-H...O hydrogen bonds between the molecules.
Application
2-Chloro-N-phenylacetamide may be used in the preparation of N,N′-(ethane-1,2-diyl)bis(2-(2-oxo-2-(phenylamino)ethoxy)benzamide), an amide podand. It may also be used to prepare phenylacetamide-based Schiff base ligands by reacting with corresponding hydrazones.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Analytical and bioanalytical chemistry, 379(3), 368-374 (2004-05-01)
Body burdens from exposures to pesticides may be estimated from urinary analyses of pesticide parent/metabolite concentrations. Pesticide applicators and others are often exposed to numerous unrelated pesticides, either sequentially or simultaneously. Classically, body burdens of pesticides are analyzed using chemical/instrumental
2-Chloro-N-phenylacetamide
Gowda BT, et al.
Acta Crystallographica Section E, Structure Reports Online, 64(6), o987-o987 (2008)
Synthesis and Fluorescence Properties of Eu3+, Tb3+ Complexes with Schiff Base Derivatives.
Liu Y, et al.
Journal of Fluorescence, 26(2), 567-576 (2016)
J D Vargo
Analytical chemistry, 70(13), 2699-2703 (1998-07-17)
An analytical method is presented which permits qualitative and quantitative analysis of sulfonic acid degradates of three chloroacetanilide herbicides (acetochlor, alachlor, and metolachlor) and one chloroacetamide herbicide (dimethenamid) in groundwater at trace levels with determination by LC/MS/MS. The analytes were
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